id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
amwa-156	Schindler, Thomas	The Making of the Good Lay Summary Practice Guidance: A Multi-Stakeholder Document That Was Adopted Into Regulation: An Interview with Dr Ingrid Klingmann	2022	5	.pdf	application/pdf	3755	189	49	Lay summaries are now mandated for all clinical trials in the European Union (EU) based on European Clinical Trial Regulation (536/2014). Its devel- opment had been initiated by a group of enthusiasts who wanted to provide guidance on how to plan, write, trans- late, and disseminate lay summaries and on how to best involve patients into the process.	cache/amwa-156.pdf	txt/amwa-156.txt